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Synthesis and fungicidal activity of novel 1,3‐disubstituted 1H‐diazirine derivatives
Author(s) -
Eliazyan Karine A.,
Avetisyan Frunze V.,
Jivanshiryan Tamara L.,
Pivazyan Vergush A.,
Ghazaryan Emma A.,
Shahbazyan Lusya V.,
Harutyunyan Siranush V.,
Yengoyan Aleksandr P.
Publication year - 2011
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.524
Subject(s) - chemistry , reagent , alkylation , yield (engineering) , proton nmr , sulfanyl , medicinal chemistry , molar ratio , diazirine , sulfur , methyllithium , mass spectrum , organic chemistry , photochemistry , ion , catalysis , materials science , metallurgy
A convenient method for synthesis of novel 1‐[pyrimidinyl], 1‐[1,3,5‐triazin‐2‐carbonyl], and 1‐[thiazol‐5‐carbonyl] derivatives of 3‐thioxo‐diaziridine 1 , 3 , 5 , and 7 from corresponding hydrazides, CS2, and KOH is elaborated. The highest reaction yield was observed when these initial reagents were taken in molar ratio of 1:1.7:2.0, respectively. By alkylation of compounds 1 , 3 , 5 , and 7 that proceeds exclusively at sulfur atom, the 3‐sulfanyl derivatives of 1‐[pyrimidinyl]‐, 1‐[1,3,5‐triazin‐2‐carbonyl]‐, and 1‐[thiazol‐5‐carbonyl]‐diazirines 2 , 4 , 6 , and 8 were formed. The structures of synthesized compounds were confirmed by proton and carbon nuclear magnetic resonance (NMR), mass spectra (MS), and elemental analysis. The fungicidal activities of S‐substituted derivatives were studied. Data of preliminary biological tests testify that these compounds can be of interest in search for new fungicides. J. Heterocyclic Chem., (2010).